Jea Andrew, Coscarella Ernesto, Chintagumpala Murali, Bhattacharjee Meena, Whitehead William E, Curry Daniel J, Luerssen Thomas G
Division of Pediatric Neurosurgery, Department of Neurosurgery, Texas Children's Hospital, Baylor College of Medicine, Houston, Texas, USA.
J Neurosurg Pediatr. 2010 Feb;5(2):149-54. doi: 10.3171/2009.9.PEDS09211.
Multiple metastatic brain tumors and multifocal primary brain tumors of a single histological type have been published in the adult and pediatric literature. However, the simultaneous occurrence of multiple primary brain tumors with different cell types is rare. Even more rare is the pediatric presentation of multiple primary brain tumors with different cell types. The authors describe the case of an 8-year-old boy who presented with a 2-week history of progressive headache, nausea and vomiting, and imbalance. Brain MR imaging demonstrated a heterogeneously enhancing mixed solid/cystic mass of the left cerebellar hemisphere and a larger, midline, more homogeneously enhancing lesion of the superior vermis. Spinal MR imaging was unremarkable. The patient underwent a suboccipital craniotomy and subsequent gross-total resection of both mass lesions. Pathological examination revealed the left cerebellar and superior vermian lesions to be a juvenile pilocytic astrocytoma and a medulloblastoma, respectively. The patient did well in the immediate postoperative period, was discharged home, and underwent neurooncological follow-up. To the best of the authors' knowledge, they describe the first known pediatric case in which a medulloblastoma and a juvenile pilocytic astrocytoma presented as synchronous primary brain tumors. They review the literature on multiple primary brain tumors with different histological characteristics and rehash potential mechanisms for their development.
成人和儿科文献中均已发表过关于多种转移性脑肿瘤以及单一组织学类型的多灶性原发性脑肿瘤的报道。然而,同时出现不同细胞类型的多种原发性脑肿瘤的情况较为罕见。更为罕见的是不同细胞类型的多种原发性脑肿瘤在儿科患者中的表现。作者描述了一名8岁男孩的病例,该男孩有2周进行性头痛、恶心、呕吐及平衡失调的病史。脑部磁共振成像显示左小脑半球有一个不均匀强化的混合实性/囊性肿块,以及一个更大的、位于中线的、强化更为均匀的上蚓部病变。脊髓磁共振成像未见异常。患者接受了枕下开颅手术,随后对两个肿块病变进行了全切除。病理检查显示左小脑和上蚓部病变分别为青少年型毛细胞型星形细胞瘤和髓母细胞瘤。患者术后即刻情况良好,出院回家,并接受了神经肿瘤学随访。据作者所知,他们描述了首例已知的儿科病例,其中髓母细胞瘤和青少年型毛细胞型星形细胞瘤表现为同步原发性脑肿瘤。他们回顾了关于具有不同组织学特征的多种原发性脑肿瘤的文献,并重新探讨了其发生发展的潜在机制。